Evidence map›Paper›PMID 36190543›Full record

ArticleHuman genetics2023

Large-scale pedigree analysis highlights rapidly mutating Y-chromosomal short tandem repeats for differentiating patrilineal relatives and predicting their degrees of consanguinity.

Arwin Ralf, Diego Montiel González, Dion Zandstra, Bram van Wersch, Nefeli Kousouri, Peter de Knijff, Atif Adnan, Sofie Claerhout, Mohsen Ghanbari, Maarten H D Larmuseau and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Human genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Forensic genetics in the omics era.Nature reviews. Genetics · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 3 countries.

Arwin RalfDepartment of Genetic Identification, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands. a.ralf@erasmusmc.nl.ORCID http://orcid.org/0000-0001-6052-0807
Diego Montiel GonzálezDepartment of Genetic Identification, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Dion ZandstraDepartment of Genetic Identification, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-2197-6315
Bram van WerschDepartment of Genetic Identification, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Nefeli KousouriDepartment of Genetic Identification, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Peter de KnijffForensic Laboratory for DNA Research, Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-0899-771X
Atif AdnanDepartment of Forensic Sciences, College of Criminal Justice, Naif Arab University of Security Sciences, Riyadh, Saudi Arabia.ORCID http://orcid.org/0000-0003-4537-0059
Sofie ClaerhoutForensic Biomedical Sciences, Department of Imaging and Pathology, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0003-0857-0211
Mohsen GhanbariDepartment of Epidemiology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-9476-7143
Maarten H D LarmuseauLaboratory of Human Genetic Genealogy, Department of Human Genetics, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0002-5974-7235
Manfred KayserDepartment of Genetic Identification, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands. m.kayser@erasmusmc.nl.ORCID http://orcid.org/0000-0002-4958-847X
Erasmus MC · NLLeiden University · NLNaif Arab University for Security Sciences · SAUniversity College West Flanders · BEUniversity of Antwerp · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rapidly mutating Y-chromosomal short tandem repeats (RM Y-STRs) were suggested for differentiating patrilineally related men as relevant in forensic genetics, anthropological genetics, and genetic genealogy. Empirical data are available for closely related males, while differentiation rates for more distant relatives are scarce. Available RM Y-STR mutation rate estimates are typically based on father-son pair data, while pedigree-based studies for efficient analysis requiring less samples are rare. Here, we present a large-scale pedigree analysis in 9379 pairs of men separated by 1-34 meioses on 30 Y-STRs with increased mutation rates including all known RM Y-STRs (RMplex). For comparison, part of the samples were genotyped at 25 standard Y-STRs mostly with moderate mutation rates (Yfiler Plus). For 43 of the 49 Y-STRs analyzed, pedigree-based mutation rates were similar to previous father-son based estimates, while for six markers significant differences were observed. Male relative differentiation rates from the 30 RMplex Y-STRs were 43%, 84%, 96%, 99%, and 100% for relatives separated by one, four, six, nine, and twelve meioses, respectively, which largely exceeded rates obtained by 25 standard Y-STRs. Machine learning based models for predicting the degree of patrilineal consanguinity yielded accurate and reasonably precise predictions when using RM Y-STRs. Fully matching haplotypes resulted in a 95% confidence interval of 1-6 meioses with RMplex compared to 1-25 with Yfiler Plus. Our comprehensive pedigree study demonstrates the value of RM Y-STRs for differentiating male relatives of various types, in many cases achieving individual identification, thereby overcoming the largest limitation of forensic Y-chromosome analysis.

Indexed as

Chromosomes, Human, YMicrosatellite RepeatsConsanguinityDNA FingerprintingGenetics, PopulationHaplotypesHumansMalePedigree

Identifiers

PMID36190543
PMCPMC9839801
OpenAlexW4300688474

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.